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Design, Synthesis, and Structure−Activity Relationships of a Series of 3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives as Acetylcholinesterase Inhibitors

Journal of medicinal chemistry, 2001-08, Vol.44 (17), p.2707-2718

2001

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Aminopyridazines as Acetylcholinesterase Inhibitors

Journal of medicinal chemistry, 1999-02, Vol.42 (4), p.730-741

1999

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Synthesis and Antibacterial Activity of Some Imidazo [1, 2-α]pyrimidine Derivatives

Chemical and Pharmaceutical Bulletin, 1992/05/25, Vol.40(5), pp.1170-1176

1992

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A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y5 Receptor Antagonist

Chemical and Pharmaceutical Bulletin, 2002, Vol.50(5), pp.636-639

2002

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Efficient one-step synthesis of 3-amino-6-arylpyridazines

Tetrahedron letters, 2001-03, Vol.42 (11), p.2115-2117

2001

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Synthesis of 4-Aryl-1-(4-methylpiperazin-1-yl)phthalazines by Suzuki-type Cross-coupling Reaction

Synthesis (Stuttgart), 2001, Vol.2001 (5), p.699-701

2001

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5-HT3 Antagonists Derived from Aminopyridazine-type Muscarinic M1 Agonists

Journal of medicinal chemistry, 1998-01, Vol.41 (3), p.311-317

1998

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EFFICIENT SYNTHESIS OF A SELECTIVE Y5 RECEPTOR ANTAGONIST

Synthetic communications, 2002-01, Vol.32 (11), p.1715-1719

2002

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New Procedure for the Preparation of the Tetrazole Analogue of GABA

Synthetic communications, 2000-04, Vol.30 (9), p.1587-1591

2000

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5-HT 3 Antagonists Derived from Aminopyridazine-type Muscarinic M1 Agonists

Journal of medicinal chemistry, 1998-01, Vol.41 (3), p.311-317

1998

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ChemInform Abstract: New Procedure for the Preparation of the Tetrazole Analogue of GABA

ChemInform, 2000-08, Vol.31 (33), p.no-no

2000

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Efficient Synthesis of a Selective Y5 Receptor Antagonist

ChemInform, 2002-10, Vol.33 (40), p.152-152

2002

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ChemInform Abstract: Synthesis of Substituted 3-Amino-6-arylpyridazines via Suzuki Reaction

ChemInform, 1999-10, Vol.30 (42), p.no-no

1999

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ChemInform Abstract: Synthesis of 4-Aryl-1-(4-methylpiperazin-1-yl)phthalazines by Suzuki-Type Cross-Coupling Reaction

ChemInform, 2001-08, Vol.32 (33), p.no-no

2001

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ChemInform Abstract: Efficient One-Step Synthesis of 3-Amino-6-arylpyridazines

ChemInform, 2001-06, Vol.32 (26), p.no-no

2001

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A Convenient 3‐Step Synthesis of 3‐Acetamido‐6‐arylpyridazines Directed to Novel Y 5 Receptor Antagonist

ChemInform, 2002-10, Vol.33 (41), p.152-152

2002

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ChemInform Abstract: Design, Synthesis, and Structure-Activity Relationships of a Series of 3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives as Acetylcholinesterase Inhibitors

ChemInform, 2001-12, Vol.32 (49), p.no-no

2001

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A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y5 Receptor Antagonist

ChemInform, 2002-10, Vol.33 (41), p.152-152

2002

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Design, Synthesis, and Structure−Activity Relationships of a Series of 3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives as Acetylcholinesterase Inhibitors

Aminopyridazines as Acetylcholinesterase Inhibitors

Synthesis and Antibacterial Activity of Some Imidazo [1, 2-α]pyrimidine Derivatives

A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y5 Receptor Antagonist

Efficient one-step synthesis of 3-amino-6-arylpyridazines

Synthesis of 4-Aryl-1-(4-methylpiperazin-1-yl)phthalazines by Suzuki-type Cross-coupling Reaction

5-HT3 Antagonists Derived from Aminopyridazine-type Muscarinic M1 Agonists

EFFICIENT SYNTHESIS OF A SELECTIVE Y5 RECEPTOR ANTAGONIST

New Procedure for the Preparation of the Tetrazole Analogue of GABA

5-HT 3 Antagonists Derived from Aminopyridazine-type Muscarinic M1 Agonists

ChemInform Abstract: New Procedure for the Preparation of the Tetrazole Analogue of GABA

Efficient Synthesis of a Selective Y5 Receptor Antagonist

ChemInform Abstract: Synthesis of Substituted 3-Amino-6-arylpyridazines via Suzuki Reaction

ChemInform Abstract: Synthesis of 4-Aryl-1-(4-methylpiperazin-1-yl)phthalazines by Suzuki-Type Cross-Coupling Reaction

ChemInform Abstract: Efficient One-Step Synthesis of 3-Amino-6-arylpyridazines

A Convenient 3‐Step Synthesis of 3‐Acetamido‐6‐arylpyridazines Directed to Novel Y 5 Receptor Antagonist

ChemInform Abstract: Design, Synthesis, and Structure-Activity Relationships of a Series of 3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives as Acetylcholinesterase Inhibitors

A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y5 Receptor Antagonist

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